Quinapril
- Product NDC
- 50090-5487
- 11-digit product format
- 500905487
- Labeler code
- 50090
- Product ID
- 50090-5487_51efc9f6-f1d7-4302-9906-2c73906a4867
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2014-08-01
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5487-0 | 50090548700 | 30 TABLET in 1 BOTTLE (50090-5487-0) | 30 tablet | 2021-03-11 | 0000-00-00 | No | No | Current |
| 50090-5487-1 | 50090548701 | 90 TABLET in 1 BOTTLE (50090-5487-1) | 90 tablet | 2021-03-11 | 0000-00-00 | No | No | Current |